The RNA world of fungal pathogens

Fungal pathogens execute well-defined infection programs that are intensively regulated at the posttranscriptional level. RNA biology determines the precise timing and subcellular expression of the encoded proteins. This temporal coordination is especially vital for membrane trafficking in order to synchronize the intracellular organelle network. This includes vacuole maturation, intra-and extracellular vesicle (EV) transport, protein entry into mitochondria, peroxisomes

the FERRY complex and annexin have been implicated in this process [5].In U. maydis, the scaffold protein Upa2 interacts with the poly(A)-binding protein, Pab1, to stabilize endosomal mRNA transport complexes [7].Furthermore, the C-terminus of Rrm4 contains a novel binding platform comprising 3 MLLE domains that operate in a strict hierarchy: while MLLE1 and MLLE2 serve accessory functions, MLLE3 is essential for the endosomal attachment of Rrm4 In fungal hyphae, mRNA-dependent processes drive membrane trafficking.Schematic depiction of U. maydis hyphae (left) interacting with its plant host, Zea mays (right).Distinct cellular processes within the hyphae have been marked and magnified.(A) Early endosomes act as a platform for the transport of mRNAs.Rrm4 (red) facilitates the mRNA transport by hitchhiking onto Rab5-positive early endosomes.Interactions between Rrm4, the poly (A)-binding protein, Pab1, and the FYVE domain-containing adapter protein Upa1 enable the attachment of mRNAs to early endosomes.The scaffold protein Upa2 stabilizes the transport complex.This bidirectional movement relies on motor proteins, kinesin, and dynein, traveling along antiparallel microtubules.The local translation of the cargo mRNAs like septin (blueish gray) on early endosomes is essential to generate higher-order septin filaments extending from the hyphal tip.(B) Khd4 (red) orchestrates membrane trafficking by regulating the subcellular levels of regulatory proteins crucial for this process.The RBP coordinates the destabilization of mRNAs encoding membrane trafficking regulators (gray) into an mRNA regulon through the recognition of the AUACCC motif present in their 3 0 UTRs.This mRNA decay process determines the induction kinetics of these mRNAs, fine-tuning their steady-state levels following transcriptional induction.Pacmans in bluish-gray depict mRNA decay factors.(C) Unconventional splicing of cib1 mRNA in the cytoplasm elicits the UPR, required to preserve ER homeostasis during infection.Upon ER stress, the ER membrane-localized Ire1 kinase/RNAse (red) is activated through its direct interaction with unfolded or misfolded proteins (orange) or by reduced Ire1-Bip1 interaction.This activation prompts the splicing of an intron from the cib1 mRNA (brown) in the cytoplasm.The resulting spliced cib1 mRNA is translationally active, leading to the production of the Cib1 protein (brown)-a bZIP transcription factor, which in turn, induces the expression of UPR genes to restore ER homeostasis and secretion.These include genes such as pit1, pit2, and pep1, encoding effector proteins vital for fungal infection.(D, E) Posttranscriptional regulation determines the dual targeting of peroxisomal proteins.(D) Alternative splicing of gapdh mRNA leads to the expression of an isoform containing peroxisomal targeting sequence (blue), which facilitates peroxisomal targeting after translation.The spliceosome complex is represented in red (gapdh-glyceraldehyde-3-phosphate dehydrogenase).(E) Ribosomal readthrough past stop codon (red box) of pgk1 mRNA integrates cryptic peroxisomal targeting sequence (blue) at the C-terminus, facilitating peroxisomal entry.The ribosome executing the stop-codon readthrough is depicted in red (pgk1-3-phosphoglycerate kinase).(F) Fungal mRNAs (red) encoding effector proteins are packaged within EVs as a means to transport into the host plant.The internalization of these fungal EVs into the plant host (light green) might be aided by clathrin-mediated endocytosis.Following their entry into plant cells, the delivered fungal mRNAs are subsequently translated using the plant's own translation machinery, thus outsourcing the production of fungal effector proteins within the plant for pathogenic development.In addition to RNAs, the cargoes of fungal EVs encompass proteins, and secondary metabolites, both depicted in gray.
https://doi.org/10.1371/journal.ppat.1011762.g001[8].Specifically, MLLE3 recognizes 2 PAM2-like sequences in the endosomal adaptor protein Upa1, which, through its FYVE zinc finger domain, anchors the mRNP complex to the endosome by recognizing phosphatidylinositol 3-phosphate, the characteristic lipid of early endosomes (Fig 1A).Recently, the first evidence of endosomal mRNA transport was also discovered in hyphae of Sordaria macrospora [5] suggesting that related fungal pathogens, such as Aspergillus fumigatus, may also utilize this mRNA transport process for hyphal development.

Regulation of mRNA stability determines membrane trafficking dynamics
Human pathogens such as Cryptococcus neoformans and C. albicans as well as plant pathogens such as U. maydis regulate RBP-mediated mRNA stability to control their virulence [9,10].In U. maydis, the multi-KH domain RBP Khd4 is crucial for morphology and pathogenicity [11].A transcriptome-wide target mRNA detection analysis was performed using hyperTRIBE (Targets of RBP Identification By Editing).In this method, Khd4 was fused with the hyperactive version of the heterologous RNA-editing enzyme ADAR (Adenosine Deaminase Acting on RNA), enabling the marking of target mRNAs through adenosine editing, which were subsequently identified using high-throughput sequencing.This in vivo approach, revealed that Khd4 binds mRNAs encoding regulatory proteins involved in membrane trafficking and specifically interacts with AUACCC regulatory elements in their 3 0 untranslated region (UTR) triggering degradation [10].Without this regulation, target mRNAs are stabilized, leading to a delayed response time during hyphal induction and pathological overshooting of their expression levels (Fig 1B).As a consequence, membrane trafficking dynamics are disrupted, causing aberrant vacuole biogenesis, and temporally altered hyphal polar growth.Hence, Khd4 unites target mRNAs encoding regulatory proteins into a defined membrane trafficking RNA regulon to ensure coordinated control of intracellular trafficking during hyphal growth [10].Given the significance of proper vacuole biogenesis in the development of appressoria-like infection structures in phytopathogens, the regulatory potential of Khd4 expands the influence of RBPs in affecting pathogen entry into plant hosts.

Cytoplasmic mRNA splicing coordinates UPR and ER trafficking during infection
Another tight link between RNA biology, protein, and membrane trafficking is the regulation of the unfolded protein response (UPR) mediating ER homeostasis during secretion.Unconventional splicing of cib1 mRNA occurs on the cytoplasmic surface of ER membranes and is mediated by the transmembrane kinase/RNAse Ire1 in response to ER stress (Fig 1C).The mature mRNA encodes the key bZIP transcription factor eliciting UPR.Importantly, humanand plant-pathogenic fungi rely on a functional UPR for virulence, as it plays a central role in thermotolerance, antifungal drug resistance, and proper protein secretion [12].In U. maydis, the UPR is adapted to the biotrophic lifestyle of the fungus and exerts additional virulencerelated functions that connect cellular physiology with the development and even transcriptional regulation of host-manipulating effectors.
During the pathogenic program, the UPR is specifically activated after plant invasion.This correlates with increased expression of more than 200 effectors many of which follow the classical ER-dependent secretory pathway [13].During infection, the interaction between Cib1 and the regulatory protein Clp1 promotes mutual stabilization and accumulation of both proteins [14,15].As Clp1 levels are decisive for initiating fungal proliferation [16,17], this interaction ensures elevated secretory capacities of fungal cells prior to host colonization.In parallel, the Cib1/Clp1 complex promotes modulated UPR gene expression, enabling long-term UPR activity [14].Transcriptome-wide analysis revealed comprehensive up-regulation of genes involved in membrane transport and protein processing in the ER [15], consistent with the increased demand for membrane traffic and effector delivery throughout infection.
Excessive ER stress is suppressed by the negative feedback of the UPR on the signaling network, which controls the expression of the vast majority of effector genes [13].Importantly, some effector genes are a direct target of the UPR regulator Cib1 [18] and thus may escape this global repression, arguing for an important contribution of these effectors in virulence.Indeed, 3 of the 4 directly regulated effector-related genes encode essential virulence factors (Fig 1C ; pit1, pit2, pep1) [13].Interestingly, another mode of fine-tuning UPR kinetics is found in C. neoformans.Here, binding of the pumilio-type RNA-binding Puf4 to the mRNA encoding the Cib1-like protein Hxl1 supports unconventional splicing during UPR activation and mRNA degradation during recovery from ER stress [19].In essence, RNA regulation at the level of unconventional splicing is upstream of a defined transcriptional response regulating correct ER-dependent membrane trafficking.

Diverse RNA regulation determines peroxisomal protein entry
Peroxisomes are essential organelles involved in myriad cellular processes including lipid homeostasis, reactive oxygen metabolism, and secondary metabolite production.In U. maydis, several glycolytic enzymes such as glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and 3-phosphoglycerate kinase (PGK-1) are targeted to peroxisomes through alternative splicing and translational readthrough, respectively.In both cases, the C-terminus gains a functional peroxisomal targeting sequence (Fig 1D and 1E) [20].As peroxisomal membranes are impervious to NAD + /NADH, the cryptic peroxisomal localization of these enzymes coordinates redox cycling between cytoplasm and peroxisomes.Significantly, stop-codon readthrough stands out as the predominant mechanism employed by both fungi and mammals to generate cryptic peroxisomal targeting sequences, whereby ribosomes continue translating past a termination codon to produce peroxisomal isoforms.This low rate of stop-codon readthrough rates enables the release of small but steady amounts of these enzymes to support peroxisome metabolism [21,22].For translational readthrough, both U. maydis and human cells require a specific sequence context involving the UGA stop codon followed by the dinucleotide CU [23].A recent discovery revealed another mechanism involving translation initiation with non-AUG start codons that target 6-phosphogluconate dehydrogenases of the pentose phosphate pathway to peroxisome [24].Notably, removing the peroxisomal targeting sequence from these bona fide cytosolic enzymes reduces the virulence of U. maydis, underscoring the significance of RNA regulation-dependent peroxisomal protein targeting in pathogenic development.

Extracellular vesicle-mediated transport of RNAs determines host communication
Intracellular membrane and RNA trafficking processes can influence the extracellular milieu via secretion.Pathogenic fungi secrete molecular weapons, termed effectors, to manipulate the host during infection.Extracellular RNAs (exRNAs) are emerging as a novel class of effectors that can modulate host gene expression.The phenomenon of bidirectional cross-kingdom RNAi (ckRNAi) has been particularly well documented in plant-pathogen interactions, whereby both partners secrete small RNAs (sRNAs) that silence genes in one another [25].The first sRNA effectors were discovered in Botrytis cinerea, which is loaded into AGO1-RISC of the host Arabidopsis thaliana to down-regulate plant defense-related genes [26].ckRNAi is a widespread phenomenon; sRNA effectors have been found in various other fungal, oomycetes, and even in bacterial pathogens and symbionts [25].
The routes of secretion and uptake of RNA during host-pathogen interaction are contentious, due to several possible mechanisms and a large variability between the systems.Extracellular vesicles (EVs) are one of the ubiquitous means of RNA secretion.In plant-pathogen interactions, A. thaliana sRNAs targeting B. cinerea transcripts were found associated with EVs, and DEAD-box RNA helicases and annexins have been implicated in their secretion [27].As for the uptake of exRNAs, clathrin-mediated endocytosis of fungal EVs is a likely route of fungal sRNA effector delivery, but it remains to be elucidated how these sRNAs escape endosomes and are loaded into host AGOs [25].
Besides canonical sRNAs and mRNAs, tRNAs and tRNA fragments, circular RNAs, and even rRNAs can be secreted [25].As EVs can carry much larger RNAs, there is an intriguing possibility of fungal mRNA delivery and translation into functional effector proteins in host cells (Fig 1F).EV-associated mRNAs of Paracoccidiodes brasiliensis are translation-competent, yielding protein products in vitro.A comprehensive analysis of mRNAs associated with EVs from U. maydis cultures, designed to mimic infectious hyphae, has identified several candidate mRNA effectors that meet the following criteria: relatively enriched in EVs compared to the cells and up-regulated during infection [28].As expected for a pathway parallel to conventionally secreted effectors, ER-targeted mRNAs and those encoding proteins with signal peptides were underrepresented in EVs.Notable among mRNA effector candidates are those encoding metabolic enzymes, which may reflect the capacity of U. maydis to reprogram the host metabolism [28].The biological relevance of these diverse RNA species from pathogens remains to be discovered, whether they serve as virulence factors or elicitors of host immunity during interaction with the host, or alternatively as mediators of intraspecies communication between fungal cells.

Conclusions and future directions
Studying U. maydis as a model pathogen reveals an intricate interplay between RNA biology and membrane trafficking.The regulation of RNA processes like splicing, localization, translation, and stability, precisely governs the exact translation levels of virulence factors.This investigation unveils a novel connection involving small GTPase regulation, septins, UPR, peroxisomal function, and the pathogen RNA trafficking to host cells.
Understanding RNA biology is essential for studying the fundamental biology of fungal pathogens.A recent demonstration showcased that in Magnoporthe oryzae tRNA modification and codon usage regulate unconventional secretion of protein effectors [29].Advances in techniques like iCLIP and HyperTRIBE have propelled the investigation of RBPs in fungal pathogens, enabling detailed mapping of RBP-binding across the transcriptome.HyperTRIBE, in particular, offers a unique avenue to delve into the host-pathogen interaction interface at the RNA level.These methods promise discoveries that advance fungal pathogenesis understanding, fostering novel antifungal therapies.

Fig 1 .
Fig 1.In fungal hyphae, mRNA-dependent processes drive membrane trafficking.Schematic depiction of U. maydis hyphae (left) interacting with its plant host, Zea mays (right).Distinct cellular processes within the hyphae have been marked and magnified.(A) Early endosomes act as a platform for the transport of mRNAs.Rrm4 (red) facilitates the mRNA transport by hitchhiking onto Rab5-positive early endosomes.Interactions between Rrm4, the poly (A)-binding protein, Pab1, and the FYVE domain-containing adapter protein Upa1 enable the attachment of mRNAs to early endosomes.The scaffold protein Upa2 stabilizes the transport complex.This bidirectional movement relies on motor proteins, kinesin, and dynein, traveling along antiparallel microtubules.The local translation of the cargo mRNAs like septin (blueish gray) on early endosomes is essential to generate higher-order septin filaments extending from the hyphal tip.(B) Khd4 (red) orchestrates membrane trafficking by regulating the subcellular levels of regulatory proteins crucial for this process.The RBP coordinates the destabilization of mRNAs encoding membrane trafficking regulators (gray) into an mRNA regulon through the recognition of the AUACCC motif present in their 3 0 UTRs.This mRNA decay process determines the induction kinetics of these mRNAs, fine-tuning their steady-state levels following transcriptional induction.Pacmans in bluish-gray depict mRNA decay factors.(C) Unconventional splicing of cib1 mRNA in the cytoplasm elicits the UPR, required to preserve ER homeostasis during infection.Upon ER stress, the ER membrane-localized Ire1 kinase/RNAse (red) is activated through its direct interaction with unfolded or misfolded proteins (orange) or by reduced Ire1-Bip1 interaction.This activation prompts the splicing of an intron from the cib1 mRNA (brown) in the cytoplasm.The resulting spliced cib1 mRNA is translationally active, leading to the production of the Cib1 protein (brown)-a bZIP transcription factor, which in turn, induces the expression of UPR genes to restore ER homeostasis and secretion.These include genes such as pit1, pit2, and pep1, encoding effector proteins vital for fungal infection.(D, E) Posttranscriptional regulation determines the dual targeting of peroxisomal proteins.(D) Alternative splicing of gapdh mRNA leads to the expression of an isoform containing peroxisomal targeting sequence (blue), which facilitates peroxisomal targeting after translation.The spliceosome complex is represented in red (gapdh-glyceraldehyde-3-phosphate dehydrogenase).(E) Ribosomal readthrough past stop codon (red box) of pgk1 mRNA integrates cryptic peroxisomal targeting sequence (blue) at the C-terminus, facilitating peroxisomal entry.The ribosome executing the stop-codon readthrough is depicted in red (pgk1-3-phosphoglycerate kinase).(F) Fungal mRNAs (red) encoding effector proteins are packaged within EVs as a means to transport into the host plant.The internalization of these fungal EVs into the plant host (light green) might be aided by clathrin-mediated endocytosis.Following their entry into plant cells, the delivered fungal mRNAs are subsequently translated using the plant's own translation machinery, thus outsourcing the production of fungal effector proteins within the plant for pathogenic development.In addition to RNAs, the cargoes of fungal EVs encompass proteins, and secondary metabolites, both depicted in gray.